Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2609-2014 — AB SCIEX API 3200MD" LC/MS/MS System with software: MultiQuantMD 3.0In vitro diagnostic to identify inorganic or organic compounds (e.g., lead, mercury, and drugs) in human specimens Part Number 5024543.

U.S. FDA — Device Enforcement · United States · 2014-07-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2609-2014
Date of alert
2014-07-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ab Sciex
Product category
device
Product type
Devices
Reported risk: Software- AB SCIEX API 3200MD LC/MS/MS SYSTEM with MultiQuantMD 3.0 software may provide incorrect data for patient diagnosis
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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